Canonical Allele Identifier: PA2825747269
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 624138
ClinVar RCV Id: RCV000762271
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Gly531Arg
CA347217527
NM_001130976.2:c.1591G>C